Chiral compounds of essential oils. Part XI. Simultaneous stereoanalysis of lavandula oil constituents
✍ Scribed by Peter Kreis; Armin Mosandl
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 420 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0882-5734
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Enantioselective multidimensional gas chromatography using the column combination Carbowax 20 M/heptakis‐(2,3‐di‐O‐acetyl‐6‐O‐tert‐butyldimethylsilyl)‐β‐cyclodextrin in OV 1701‐vinyl allows the simultaneous stereodifferentiation of trans‐ and cis‐linalol oxides (furanoid), camphor, octan‐3‐ol, oct‐1‐en‐3‐ol, linalyl acetate, lavandulol, terpinen‐4‐ol and linalol. The method is applied to commercially available as well as self‐prepared essential oils of Lavandula species. Chirality evaluation is discussed in view of quality assessment of these essential oils.
📜 SIMILAR VOLUMES
## Abstract Enantiomeric diterpene hydrocarbons were isolated from different plants and identified by mass spectrometric and NMR investigations. All enantiomeric pairs could be resolved by capillary gas chromatography using either heptakis(2,6‐di‐__O__‐methyl‐3‐__O__‐pen‐tyl)‐β‐cyclodextrin or hept
## Abstract Using a dual column gas chromatograph equipped with two capillary columns coated with heptakis(6‐__O__‐methyl‐2,3‐di‐__O__‐pentyl)‐β‐cyclodextrin (6‐me‐2,3‐pe‐β‐CD) and octakis(6‐__O__‐methyl‐2,3‐di‐__O__‐pentyl)‐γ‐cyclodextrin (6‐me‐2,3‐pe‐γ‐CD), respectively, all important olefinic mo